Tracking Clathrin Coated Pits with a Multiple Hypothesis Based Method

Cellular processes are crucial for cells to survive and function properly. To study their underlying mechanisms quantitatively with fluorescent live cell microscopy, it is necessary to track a large number of particles involved in these processes. In this paper, we present a method to automatically track particles, called clathrin coated pits (CCPs), which are formed in clathrin mediated endocytosis (CME). The tracking method is developed based on a MAP framework, and it consists of particle detection and trajectory estimation. To detect particles in 2D images and take account of Poisson noise, a Gaussian mixture model is fitted to image data, for which initial parameters are provided by a combination of image filtering and histogram based thresholding methods. A multiple hypothesis based algorithm is developed to estimate the trajectories based on detection data. To use the current knowledge about CCPs, their properties of motion and intensity are considered in our models. The tracking method is evaluated on synthetic data and real data, and experimental results show that it has high accuracy and is in good agreement with manual tracking.

[1]  D. Reid An algorithm for tracking multiple targets , 1978, 1978 IEEE Conference on Decision and Control including the 17th Symposium on Adaptive Processes.

[2]  Anand Rangarajan,et al.  The Softassign Procrustes Matching Algorithm , 1997, IPMI.

[3]  P. Camilli,et al.  Accessory factors in clathrin-dependent synaptic vesicle endocytosis , 2000, Nature Reviews Neuroscience.

[4]  Cor J. Veenman,et al.  Resolving Motion Correspondence for Densely Moving Points , 2001, IEEE Trans. Pattern Anal. Mach. Intell..

[5]  P. Sorger,et al.  Automatic fluorescent tag detection in 3D with super‐resolution: application to the analysis of chromosome movement , 2002, Journal of microscopy.

[6]  Gaudenz Danuser,et al.  Reliable Tracking of Large Scale Dense Antiparallel Particle Motion for Fluorescence Live Cell Imaging , 2005, 2005 IEEE Computer Society Conference on Computer Vision and Pattern Recognition (CVPR'05) - Workshops.

[7]  B. C. Carter,et al.  Tracking single particles: a user-friendly quantitative evaluation , 2005, Physical biology.

[8]  P. Koumoutsakos,et al.  Feature point tracking and trajectory analysis for video imaging in cell biology. , 2005, Journal of structural biology.

[9]  Aubrey B. Poore,et al.  Some assignment problems arising from multiple target tracking , 2006, Math. Comput. Model..

[10]  M. Shah,et al.  Object tracking: A survey , 2006, CSUR.

[11]  J. Zerubia,et al.  Gaussian approximations of fluorescence microscope point-spread function models. , 2007, Applied optics.

[12]  Wiro J. Niessen,et al.  ADVANCED PARTICLE FILTERING FOR MULTIPLE OBJECT TRACKING IN DYNAMIC FLUORESCENCE MICROSCOPY IMAGES , 2007, 2007 4th IEEE International Symposium on Biomedical Imaging: From Nano to Macro.

[13]  X. Zhuang,et al.  Virus trafficking – learning from single-virus tracking , 2007, Nature Reviews Microbiology.

[14]  K. Jaqaman,et al.  Robust single particle tracking in live cell time-lapse sequences , 2008, Nature Methods.

[15]  Jing Zhang,et al.  Framework for Performance Evaluation of Face, Text, and Vehicle Detection and Tracking in Video: Data, Metrics, and Protocol , 2009, IEEE Transactions on Pattern Analysis and Machine Intelligence.